<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>51</viewCount><searchCount>0</searchCount></scores><additional><submitter>Belizaire R</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>969-979</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6457231</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(7)</volume><pubmed_abstract>Chronic graft-versus-host disease (cGVHD) affects >50% of hematopoietic stem cell transplant patients. Extracorporeal photopheresis (ECP), an immunomodulatory therapy, provides clinical benefit in steroid-refractory (SR) cGVHD, possibly via regulatory T (Treg) and natural killer (NK) cell expansion. We demonstrated that low-dose interleukin-2 (IL2) led to clinical improvement in SR-cGVHD and stimulated preferential Treg and NK-cell expansion with minimal effect on conventional T (Tcon) cells. We evaluated the effect of ECP (weeks 1-16) plus IL2 (1 × 106 IU/m2, weeks 9-16) in 25 adult patients with SR-cGVHD in a prospective phase 2 trial. Objective responses occurred in 29% and 62% of evaluable patients at weeks 8 (ECP alone) and 16 (ECP plus IL2), respectively. Eight weeks of ECP alone was associated with a marked decline in CD4+ Tcon (P = .03) and CD8+ T cells (P = .0002), with minimal change in Treg cells, Treg:Tcon cell ratio, or NK cells. Adding IL2 induced an increase in Treg cells (P &lt; .05 at weeks 9-16 vs week 8), Treg:Tcon cell ratio (P &lt; .0001 at weeks 9-16 vs week 8), and NK cells (P &lt; .05 at weeks 9-16 vs week 8). Patients responding to ECP alone had significantly fewer CD4+ Tcon and CD8+ T cells at baseline compared with patients who responded after IL2 addition and patients who did not respond; neither Treg nor NK cells were associated with response to ECP alone. Altogether, ECP plus IL2 is safe and effective in patients with SR-cGVHD. ECP and IL2 have distinct immunologic effects, suggesting different therapeutic mechanisms of action. This trial was registered at www.clinicaltrials.gov as #NCT02340676.</pubmed_abstract><journal>Blood advances</journal><pubmed_title>Efficacy and immunologic effects of extracorporeal photopheresis plus interleukin-2 in chronic graft-versus-host disease.</pubmed_title><pmcid>PMC6457231</pmcid><funding_grant_id>P01 CA142106</funding_grant_id><funding_grant_id>P01 AI056299</funding_grant_id><funding_grant_id>R01 HL118979</funding_grant_id><funding_grant_id>R01 CA183559</funding_grant_id><funding_grant_id>R01 CA183560</funding_grant_id><funding_grant_id>P01 CA229092</funding_grant_id><pubmed_authors>Belizaire R</pubmed_authors><pubmed_authors>Alyea EP</pubmed_authors><pubmed_authors>Blazar BR</pubmed_authors><pubmed_authors>Hipolito E</pubmed_authors><pubmed_authors>Whangbo J</pubmed_authors><pubmed_authors>Kim HT</pubmed_authors><pubmed_authors>Nikiforow S</pubmed_authors><pubmed_authors>Fields MJ</pubmed_authors><pubmed_authors>Ritz J</pubmed_authors><pubmed_authors>Koreth J</pubmed_authors><pubmed_authors>Cutler CS</pubmed_authors><pubmed_authors>Poryanda SJ</pubmed_authors><pubmed_authors>Kubo T</pubmed_authors><pubmed_authors>Antin JH</pubmed_authors><pubmed_authors>Armand P</pubmed_authors><pubmed_authors>Mirkovic NV</pubmed_authors><pubmed_authors>Reynolds CG</pubmed_authors><pubmed_authors>Soiffer RJ</pubmed_authors><pubmed_authors>Savage WJ</pubmed_authors><pubmed_authors>Ho VT</pubmed_authors><view_count>51</view_count></additional><is_claimable>false</is_claimable><name>Efficacy and immunologic effects of extracorporeal photopheresis plus interleukin-2 in chronic graft-versus-host disease.</name><description>Chronic graft-versus-host disease (cGVHD) affects >50% of hematopoietic stem cell transplant patients. Extracorporeal photopheresis (ECP), an immunomodulatory therapy, provides clinical benefit in steroid-refractory (SR) cGVHD, possibly via regulatory T (Treg) and natural killer (NK) cell expansion. We demonstrated that low-dose interleukin-2 (IL2) led to clinical improvement in SR-cGVHD and stimulated preferential Treg and NK-cell expansion with minimal effect on conventional T (Tcon) cells. We evaluated the effect of ECP (weeks 1-16) plus IL2 (1 × 106 IU/m2, weeks 9-16) in 25 adult patients with SR-cGVHD in a prospective phase 2 trial. Objective responses occurred in 29% and 62% of evaluable patients at weeks 8 (ECP alone) and 16 (ECP plus IL2), respectively. Eight weeks of ECP alone was associated with a marked decline in CD4+ Tcon (P = .03) and CD8+ T cells (P = .0002), with minimal change in Treg cells, Treg:Tcon cell ratio, or NK cells. Adding IL2 induced an increase in Treg cells (P &lt; .05 at weeks 9-16 vs week 8), Treg:Tcon cell ratio (P &lt; .0001 at weeks 9-16 vs week 8), and NK cells (P &lt; .05 at weeks 9-16 vs week 8). Patients responding to ECP alone had significantly fewer CD4+ Tcon and CD8+ T cells at baseline compared with patients who responded after IL2 addition and patients who did not respond; neither Treg nor NK cells were associated with response to ECP alone. Altogether, ECP plus IL2 is safe and effective in patients with SR-cGVHD. ECP and IL2 have distinct immunologic effects, suggesting different therapeutic mechanisms of action. This trial was registered at www.clinicaltrials.gov as #NCT02340676.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2024-02-15T22:13:00.239Z</modification><creation>2019-06-05T16:19:52Z</creation></dates><accession>S-EPMC6457231</accession><cross_references><pubmed>30936057</pubmed><doi>10.1182/bloodadvances.2018029124</doi></cross_references></HashMap>